| 论文题目: | The characteristics of nucleocytoplasmic transport of H1N1 influenza A viruses nuclear export protein (NEP) |
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| 作者: | Gao Shengyan, Wang Shanshan, Cao Shuai, Sun Lei, Li Jing, Bi Yuhai, George F Gao, Liu Wenjun* |
| 联系作者: | Liu Wenjun* |
| 刊物名称: | J Virol |
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| 年份: | 2014 |
| 影响因子: | 4.893 |
| 论文下载: | 下载地址 |
| 摘要: | The influenza A virus nuclear export protein (NEP) plays crucial roles in the nuclear export of the viral ribonucleoprotein complex through the CRM1-mediated cellular protein transport system. However, the detailed mechanism of NEP nucleocytoplasmic trafficking remain incompletely understood. Here, we investigated the subcellular localization of NEP from two strains of H1N1 influenza A virus and found that 2009 swine-origin H1N1 influenza A virus A/California/04/2009 (CA04) NEP displayed a distinct cellular distribution pattern, forming unique nuclear aggregates, compared to A/WSN/33 (H1N1) (WSN) NEP. Characterization of the nucleocytoplasmic transport pathways of these two NEPs showed that they both enter the nucleus by passive diffusion but are exported through the nuclear export receptor chromosome region maintenance 1 (CRM1)-mediated pathway with different efficiencies. The two identified NESs on both NEPs functioned similarly despite differences in their amino acid sequences. Using a two-hybrid assay, we confirmed that the CA04 NEP interacts less efficiently with CRM1, and a threonine residue at position 48 is responsible for the nuclear aggregation. The present study revealed the dissimilarity in subcellular NEP transport processes between the 2009 pandemic (H1N1) influenza A virus CA04 and lab-adapted H1N1 virus WSN and uncovered the mechanism for this difference. IMPORTANCE: Because the efficiency of the nucleocytoplasmic transport of viral components is often correlated with the viral RNA polymerase activity, propagation, and host range of influenza viruses, the present study investigated the subcellular localization of NEP from two strains of H1N1 influenza virus. We found that both the NEPs of A/California/04/2009 (H1N1) (CA04) and A/WSN/33 (H1N1) (WSN) enter the nucleus by passive diffusion but are exported with different efficiencies, which was caused by weaker binding activity between the CA04 NEP and CRM1. The results of the present study revealed characteristics of the nuclear import and export pathways of NEP and mechanism for the difference in cellular distribution of NEP between two H1N1 strains. |
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